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Progress Update Advisory Committee to Director, NIH December 5, 2008

NIH Blue Ribbon Panel to Advise on Risk Assessment for the BU National Emerging Infectious Diseases Laboratories. Progress Update Advisory Committee to Director, NIH December 5, 2008. Phase I Recommendations Regarding Supplementary Risk Assessment.

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Progress Update Advisory Committee to Director, NIH December 5, 2008

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  1. NIH Blue Ribbon Panel to Advise on Risk Assessment for the BU National Emerging Infectious Diseases Laboratories Progress Update Advisory Committee to Director, NIH December 5, 2008

  2. Phase I Recommendations Regarding Supplementary Risk Assessment • Briefed ACD in June 2008 regarding proposed scope and analytic approach for supplementary risk assessment • ACD voted to accept BRP recommendations and noted the following elements should be explicitly included: • Assessment of probability of detection of pathogen release; • Availability of vaccines and characteristics of communities, including the range of healthcare providers utilized by community members • Alternative site analyses of urban, suburban and rural areas • Community input in formulation of recommendations • NIH Director approved the recommendations regarding studies to assess risk of operating the NEIDL and authorized initiation of the studies

  3. Update on Supplementary Risk Assessment • Contract awarded in September 2008 • Broad range of infectious agents and scenarios as recommended by the ACD • Ongoing oversight of study by the Blue Ribbon Panel • Public engagement during conduct of study and public comment on draft written report in 2009 • BRP will provide ACD with an update on status of studies in June 2009

  4. Interim Status of BUMC NEIDL Operation • No BSL 3 or 4 operations during this time – pending outcome of court decisions • BUMC proposed public safety, health, and operations training in partnership with public health authorities

  5. Boston Prohibition on the Use of Recombinant DNA at BSL-4 • The City of Boston has a regulation that prohibits the use of recombinant DNA technology requiring BSL-4 containment • The Panel and the NIH emphasize that the research will fully comply with any and all Boston City regulations, including the current prohibition on recombinant DNA use at BSL-4 • Boston University has affirmed that all research at their institution will be in compliance with this City of Boston regulation

  6. Phase II Tasks • Advise NIH on strategies to address local community relations and communications regarding the BUMC NEIDL as part of the supplemental risk assessment • Develop principles and identify best practices in the context of a national research resource

  7. Panel Approach • NIH Blue Ribbon Panel Meetings devoted to community engagement topics • Briefings regarding local oversight frameworks and community engagement • Regional and National Biocontainment Laboratories funded through the NIAID/NIH Emerging Infectious Diseases and Biodefense Program • Boston University • Boston Public Health Commission

  8. BRP Meetings with the Community • May 16, 2008 (Boston) • Present the BRP charge and proposed approach to supplementary risk assessment • July 16, 2008 (Bethesda) • Invited members of Boston community, Boston city officials, community researchers, and social justice advocates • Explored case studies on community engagements and environmental justice • Roundtable discussion of how to effectively engage communities • October 14, 2008 (Boston) • Engaged community members in planning of meeting and outreach efforts • Evening meeting in local community hall to: • Present and seek community input on draft principles and best practices for community engagement • Hear general comments and perspectives from community members

  9. Principles and Best Practices for Public and Local Community Relations and Communications • Build on existing measures with the goal of achieving best practices • Apply to Regional and National Biocontainment Laboratories funded by the NIH • NOTE: These principles will apply to the NEIDL only if ongoing supplementary risk assessment studies, court cases, and Massachusetts state authorities point to the acceptability of conducting high- and maximum-containment research conditions • Draft principles are generally applicable to other high- and maximum-containment labs • Implementation of principles will be left up to individual institutions

  10. Draft Principles • Rigorous, balanced, and transparent local institutional biosafety review of proposed biocontainment research at high- and maximum-containment research at NIH-funded RBLs and NBLs • Maximal transparency regarding facility operation, nature of research, and oversight of research • Community engagement • Appropriate technical expertise • Engagement of the local public health authorities • Ongoing operations oversight

  11. Best Practices • Rigorous, balanced, transparent local institutional biosafety review and oversight of high- and maximum-containment research • Community liaison activities to promote openness and transparency with respect to the research agenda of the institution • Communications plan regarding phase-in of research operations

  12. Best Practices • Rigorous, balanced, and transparent local institutional review and oversight of high- and maximum-containment research should embody the following principles: • Appropriate technical expertise • Periodic review of research • Ongoing operations oversight, including laboratory inspections and systems testing • Maximal transparency regarding facility operation and the nature and oversight of research • Community engagement

  13. Rigorous, Balanced, Transparent Local Institutional Review • BRP recommends that all high- and maximum-containment infectious disease research conducted in Regional and National Biocontainment Laboratories funded by the NIH be reviewed, approved, and overseen by an institutional body • At least two non-institutional members who can represent the interests of the local community • Institutional Biosafety Committees offer an example of such an institutional review bodies

  14. Rigorous, Balanced, Transparent Local Institutional Review • Currently, IBC review mandated only for recombinant DNA research • Review includes: • Community representatives • Biosafety and scientific expertise • Authority to approve/disapprove rDNA protocols • Ongoing oversight throughout life of research project • Minutes publicly available • Many institutions nonetheless have established local review and oversight mechanisms for work with non-recombinant infectious agents

  15. Best Practices • Community liaison activities to promote openness and transparency with respect to the research agenda of the institution • These activities should be integrative and offer opportunities for: • Input from community about impact of lab • Communication to the community regarding lab operations • Community education about research programs and public health benefits of research

  16. Best Practices • Communications plan regarding phase-in of research operations • Regional and National Biocontainment Laboratories funded by the NIH should communicate specific information regarding safeguards and precautions often utilized in phasing in research operations • Conduct of low-containment research under maximum containment conditions for training • Ample technical expertise to assess performance of building systems and readiness for operation • Institutions should inform their communities and local public health authorities about plans for transitioning to a fully operational high – and maximum-containment laboratory

  17. Discussion

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